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Redman/Chief Power Chair

FDA UDI

Class II (US FDA UDI)

by Chief Power Chair, Llc

Identity

Trade Name
Redman/Chief Power Chair FDA UDI
Generic Name
Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible FDA UDI
Model / Reference
Chief 107-ZRx FDA UDI

Identifiers

Primary DI / UDI-DI
00863444000308 FDA UDI
510(k) Number
K940919 FDA UDI
FDA Product Code
IPL FDA UDI
GMDN Term
Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible

Redman/Chief Power Chair by Chief Power Chair, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Chief Power Chair, Llc

Sources (1)

  • FDA UDI 671cb18d-9d15-44da-b8b8-d3b653b0a4db 33 fields · synced Jun 8, 2026